FDA 510(k) Application Details - K024020

Device Classification Name	Light, Ultraviolet, Dermatological   More FDA Info for this Device
510(K) Number	K024020
Device Name	Light, Ultraviolet, Dermatological
Applicant	THERALIGHT, INC. 2794 LOKER AVE. WEST,SUITE 105 CARLSBAD, CA 92008-6616 US Other 510(k) Applications for this Company
Contact	KEVIN E DALY Other 510(k) Applications for this Contact
Regulation Number	878.4630   More FDA Info for this Regulation Number
Classification Product Code	FTC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/05/2002
Decision Date	01/17/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review